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利用高分辨率熔解扩增分析检测非小细胞肺癌患者细胞学标本中的表皮生长因子受体基因突变

Detection of epidermal growth factor receptor gene mutations in cytology specimens from patients with non-small cell lung cancer utilising high-resolution melting amplicon analysis.

作者信息

Smith G D, Chadwick B E, Willmore-Payne C, Bentz J S

机构信息

Institute for Clinical and Experimental Pathology, Associated Regional and University Pathologists (ARUP) Laboratories, Inc., Salt Lake City, Utah, USA.

出版信息

J Clin Pathol. 2008 Apr;61(4):487-93. doi: 10.1136/jcp.2007.051425. Epub 2007 Oct 1.

Abstract

BACKGROUND

Activating epidermal growth factor receptor (EGFR) mutations have been implicated in non-small cell lung cancer (NSCLC), and have also been clinically correlated with patient sensitivity to targeted EGFR inhibitors.

AIM

To describe a technique for determining EGFR mutation status on archival fine needle aspirate (FNA) specimens from advanced NSCLC patients.

METHODS

Eleven archival FNA slides from patients with advanced NSCLC were examined for diagnostic material to identify tumour cell-enriched regions. EGFR mutation status was determined using a slide-scrape DNA extraction protocol of selected tumour cell regions on the smear slides, followed by real time PCR and high resolution melt analysis (HRMAA) of EGFR exons 18, 19, 20, and 21, followed by sequence analysis.

RESULTS

All DNA samples were successfully amplified by PCR. Three adenocarcinoma patient samples contained EGFR mutations in exon 19 (L747-P753insS). One of the three had an additional exon 19 mutation (A755D).

CONCLUSIONS

Archival cytology slides from patients with NSCLC can be used to determine EGFR mutation status by PCR, HRMAA, and sequencing. The ability to use archival cytology slides greatly increases the potential material available for molecular analysis in diagnosis and selection of patients for targeted therapeutic agents.

摘要

背景

激活型表皮生长因子受体(EGFR)突变与非小细胞肺癌(NSCLC)有关,并且在临床上也与患者对EGFR靶向抑制剂的敏感性相关。

目的

描述一种用于确定晚期NSCLC患者存档细针穿刺抽吸(FNA)标本中EGFR突变状态的技术。

方法

检查11例晚期NSCLC患者的存档FNA玻片,寻找诊断材料以识别富含肿瘤细胞的区域。使用涂片玻片上选定肿瘤细胞区域的玻片刮取DNA提取方案确定EGFR突变状态,随后对EGFR第18、19、20和21外显子进行实时PCR和高分辨率熔解分析(HRMAA),然后进行序列分析。

结果

所有DNA样本均通过PCR成功扩增。3例腺癌患者样本在第19外显子中存在EGFR突变(L747-P753insS)。其中1例在第19外显子还有另一个突变(A755D)。

结论

NSCLC患者的存档细胞学玻片可用于通过PCR、HRMAA和测序确定EGFR突变状态。使用存档细胞学玻片的能力大大增加了可用于分子分析以诊断和选择靶向治疗药物患者的潜在材料。

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